Natalizumab treatment of multiple sclerosis — a Danish nationwide study with 13 years of follow-up

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Natalizumab treatment of multiple sclerosis — a Danish nationwide study with 13 years of follow-up. / Buron, Mathias Due; Christensen, Jeppe Romme; Pontieri, Luigi; Joensen, Hanna; Kant, Matthias; Rasmussen, Peter Vestergaard; Sellebjerg, Finn; Sørensen, Per Soelberg; Bech, Danny; Magyari, Melinda.

I: Multiple Sclerosis and Related Disorders, Bind 74, 104713, 2023.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Buron, MD, Christensen, JR, Pontieri, L, Joensen, H, Kant, M, Rasmussen, PV, Sellebjerg, F, Sørensen, PS, Bech, D & Magyari, M 2023, 'Natalizumab treatment of multiple sclerosis — a Danish nationwide study with 13 years of follow-up', Multiple Sclerosis and Related Disorders, bind 74, 104713. https://doi.org/10.1016/j.msard.2023.104713

APA

Buron, M. D., Christensen, J. R., Pontieri, L., Joensen, H., Kant, M., Rasmussen, P. V., Sellebjerg, F., Sørensen, P. S., Bech, D., & Magyari, M. (2023). Natalizumab treatment of multiple sclerosis — a Danish nationwide study with 13 years of follow-up. Multiple Sclerosis and Related Disorders, 74, [104713]. https://doi.org/10.1016/j.msard.2023.104713

Vancouver

Buron MD, Christensen JR, Pontieri L, Joensen H, Kant M, Rasmussen PV o.a. Natalizumab treatment of multiple sclerosis — a Danish nationwide study with 13 years of follow-up. Multiple Sclerosis and Related Disorders. 2023;74. 104713. https://doi.org/10.1016/j.msard.2023.104713

Author

Buron, Mathias Due ; Christensen, Jeppe Romme ; Pontieri, Luigi ; Joensen, Hanna ; Kant, Matthias ; Rasmussen, Peter Vestergaard ; Sellebjerg, Finn ; Sørensen, Per Soelberg ; Bech, Danny ; Magyari, Melinda. / Natalizumab treatment of multiple sclerosis — a Danish nationwide study with 13 years of follow-up. I: Multiple Sclerosis and Related Disorders. 2023 ; Bind 74.

Bibtex

@article{39e944a62e04485d8ff0977a8331e595,
title = "Natalizumab treatment of multiple sclerosis — a Danish nationwide study with 13 years of follow-up",
abstract = "Background: Natalizumab is a widely used high-efficacy treatment in multiple sclerosis (MS). Real-world evidence regarding long-term effectiveness and safety is warranted. We performed a nationwide study evaluating prescription patterns, effectiveness, and adverse events. Methods: A nationwide cohort study using the Danish MS Registry. Patients initiating natalizumab between June 2006 and April 2020 were included. Patient characteristics, annualized relapse rates (ARRs), confirmed Expanded Disability Status Scale (EDSS) score worsening, MRI activity (new/enlarging T2- or gadolinium-enhancing lesions), and reported adverse events were evaluated. Further, prescription patterns and outcomes across different time periods (“epochs”) were analysed. Results: In total, 2424 patients were enrolled, with a median follow-up time of 2.7 years (interquartile range (IQR) 1.2–5.1). In recent epochs, patients were younger, had lower EDSS scores, had fewer pre-treatment relapses and were more often treatment na{\"i}ve. At 13 years of follow-up, 36% had a confirmed EDSS worsening. On-treatment ARR was 0.30, corresponding to a 72% reduction from pre-initiation. MRI activity was rare, 6.8% had activity within 2–14 months from treatment start, 3.4% within 14–26 months, and 2.7% within 26–38 months. Approximately 14% of patients reported adverse events, with cephalalgia constituting the majority. During the study, 62.3% discontinued treatment. Of these, the main cause (41%) was due to JCV antibodies, while discontinuations due to disease activity (9%) or adverse events (9%) were less frequent. Conclusion: Natalizumab is increasingly used earlier in the disease course. Most patients treated with natalizumab are clinically stable with few adverse events. JCV antibodies constitute the main cause for discontinuation.",
keywords = "Multiple sclerosis, Natalizumab, Observational study, Treatment, Treatment outcome",
author = "Buron, {Mathias Due} and Christensen, {Jeppe Romme} and Luigi Pontieri and Hanna Joensen and Matthias Kant and Rasmussen, {Peter Vestergaard} and Finn Sellebjerg and S{\o}rensen, {Per Soelberg} and Danny Bech and Melinda Magyari",
note = "Publisher Copyright: {\textcopyright} 2023 The Author(s)",
year = "2023",
doi = "10.1016/j.msard.2023.104713",
language = "English",
volume = "74",
journal = "Multiple Sclerosis and Related Disorders",
issn = "2211-0348",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Natalizumab treatment of multiple sclerosis — a Danish nationwide study with 13 years of follow-up

AU - Buron, Mathias Due

AU - Christensen, Jeppe Romme

AU - Pontieri, Luigi

AU - Joensen, Hanna

AU - Kant, Matthias

AU - Rasmussen, Peter Vestergaard

AU - Sellebjerg, Finn

AU - Sørensen, Per Soelberg

AU - Bech, Danny

AU - Magyari, Melinda

N1 - Publisher Copyright: © 2023 The Author(s)

PY - 2023

Y1 - 2023

N2 - Background: Natalizumab is a widely used high-efficacy treatment in multiple sclerosis (MS). Real-world evidence regarding long-term effectiveness and safety is warranted. We performed a nationwide study evaluating prescription patterns, effectiveness, and adverse events. Methods: A nationwide cohort study using the Danish MS Registry. Patients initiating natalizumab between June 2006 and April 2020 were included. Patient characteristics, annualized relapse rates (ARRs), confirmed Expanded Disability Status Scale (EDSS) score worsening, MRI activity (new/enlarging T2- or gadolinium-enhancing lesions), and reported adverse events were evaluated. Further, prescription patterns and outcomes across different time periods (“epochs”) were analysed. Results: In total, 2424 patients were enrolled, with a median follow-up time of 2.7 years (interquartile range (IQR) 1.2–5.1). In recent epochs, patients were younger, had lower EDSS scores, had fewer pre-treatment relapses and were more often treatment naïve. At 13 years of follow-up, 36% had a confirmed EDSS worsening. On-treatment ARR was 0.30, corresponding to a 72% reduction from pre-initiation. MRI activity was rare, 6.8% had activity within 2–14 months from treatment start, 3.4% within 14–26 months, and 2.7% within 26–38 months. Approximately 14% of patients reported adverse events, with cephalalgia constituting the majority. During the study, 62.3% discontinued treatment. Of these, the main cause (41%) was due to JCV antibodies, while discontinuations due to disease activity (9%) or adverse events (9%) were less frequent. Conclusion: Natalizumab is increasingly used earlier in the disease course. Most patients treated with natalizumab are clinically stable with few adverse events. JCV antibodies constitute the main cause for discontinuation.

AB - Background: Natalizumab is a widely used high-efficacy treatment in multiple sclerosis (MS). Real-world evidence regarding long-term effectiveness and safety is warranted. We performed a nationwide study evaluating prescription patterns, effectiveness, and adverse events. Methods: A nationwide cohort study using the Danish MS Registry. Patients initiating natalizumab between June 2006 and April 2020 were included. Patient characteristics, annualized relapse rates (ARRs), confirmed Expanded Disability Status Scale (EDSS) score worsening, MRI activity (new/enlarging T2- or gadolinium-enhancing lesions), and reported adverse events were evaluated. Further, prescription patterns and outcomes across different time periods (“epochs”) were analysed. Results: In total, 2424 patients were enrolled, with a median follow-up time of 2.7 years (interquartile range (IQR) 1.2–5.1). In recent epochs, patients were younger, had lower EDSS scores, had fewer pre-treatment relapses and were more often treatment naïve. At 13 years of follow-up, 36% had a confirmed EDSS worsening. On-treatment ARR was 0.30, corresponding to a 72% reduction from pre-initiation. MRI activity was rare, 6.8% had activity within 2–14 months from treatment start, 3.4% within 14–26 months, and 2.7% within 26–38 months. Approximately 14% of patients reported adverse events, with cephalalgia constituting the majority. During the study, 62.3% discontinued treatment. Of these, the main cause (41%) was due to JCV antibodies, while discontinuations due to disease activity (9%) or adverse events (9%) were less frequent. Conclusion: Natalizumab is increasingly used earlier in the disease course. Most patients treated with natalizumab are clinically stable with few adverse events. JCV antibodies constitute the main cause for discontinuation.

KW - Multiple sclerosis

KW - Natalizumab

KW - Observational study

KW - Treatment

KW - Treatment outcome

U2 - 10.1016/j.msard.2023.104713

DO - 10.1016/j.msard.2023.104713

M3 - Journal article

C2 - 37058764

AN - SCOPUS:85152124866

VL - 74

JO - Multiple Sclerosis and Related Disorders

JF - Multiple Sclerosis and Related Disorders

SN - 2211-0348

M1 - 104713

ER -

ID: 366765886